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      Regiospecific Intermolecular Aminohydroxylation of Olefins by Photoredox Catalysis.

      Chemistry (Weinheim an Der Bergstrasse, Germany)
      Wiley
      homogeneous catalysis, electron transfer, photochemistry, amination, carbocations

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          Abstract

          A simple and regiospecific aminohydroxylation of olefins by photoredox catalysis has been developed. N-protected 1-aminopyridinium salts are the key compounds and serve as amidyl radical precursors by the action of Ir photocatalysts, fac-[Ir(ppy)3] and [Ir(ppy)2 (dtbbpy)](PF6) (ppy=2-pyridylphenyl, dtbbpy=4,4'-di-tert-butyl-2,2'-bipyridine). The present photocatalytic system allows for synthesis of vicinal aminoalcohol derivatives from olefins with various functional groups under mild reaction conditions with easy handling.

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          Author and article information

          Journal
          26179746
          10.1002/chem.201501590

          homogeneous catalysis,electron transfer,photochemistry,amination,carbocations

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